Results 41 to 50 of about 7,429 (165)
Recompensation of Cirrhosis: A New Treatment‐Related Disease State
This perspective article conceptualizes recompensation of cirrhosis as a distinct treatment‐related disease state rather than mere transient clinical improvement after etiology‐directed therapy, and further proposes a four‐state classification including compensated cirrhosis, stable recompensation, unstable recompensation, and persistent decompensation
Wentao Tan +5 more
wiley +1 more source
Splenectomy is a safe and effective treatment option in selected patients with haematological disease, despite declining referrals over the last 27 years in the era of targeted therapies. Outcomes are favourable when performed laparoscopically and long‐term follow‐up demonstrates sustained haematologic benefit in surviving patients.
Salil Dutt Barrett +9 more
wiley +1 more source
Histological manifestations of vitamin A toxicity in the liver
Analysing clinicopathological data from 1960 to 2025, this study characterizes the spectrum of liver injury associated with chronic vitamin A toxicity. Hepatic stellate cell hypertrophy/hyperplasia and sinusoidal fibrosis emerge as the predominant features, providing a morphological basis for diagnosing vitamin A hepatotoxicity.
Giorgio Cazzaniga +2 more
wiley +1 more source
Giant Non-traumatic Splenic Pseudocyst Mimicking a Pancreatic Pseudocyst: A Case Report [PDF]
Splenic pseudocysts are rare non-parasitic cystic lesions of the spleen haracterised by the absence of an epithelial lining. Most occur following trauma, whereas non-traumatic splenic pseudocysts are uncommon.
Priya Dharshini Rajaram +3 more
doaj +1 more source
EHA Guidelines on the management of children and adults with hemoglobin SC disease
Abstract HbSC disease is the second most common type of sickle cell disease (SCD) in populations of African origin. Although it is often grouped together with other types of SCD, particularly sickle cell anemia (HbSS), it has unique pathophysiology and a different spectrum of laboratory and clinical features.
David C. Rees +15 more
wiley +1 more source
ABSTRACT Background TAFRO syndrome is a rare inflammatory disorder whose hepatic manifestations may mimic decompensated cirrhosis. Cases: We report two women with TAFRO syndrome associated with portal‐sinusoidal vascular disorder (PSVD), a rare cause of non‐cirrhotic portal hypertension. In both cases, liver biopsy excluded cirrhosis and confirmed PSVD.
Laura Dassy +12 more
wiley +1 more source
Aim: To objectively demonstrate the gain in blood volume and blood components following early ligation of splenic artery during splenectomy and splenorenal shunts in children with extra hepatic portal venous obstruction (EHPVO).
Gazula Suhasini +4 more
doaj
ABSTRACT Aim Steatotic liver disease (SLD) encompasses a heterogeneous spectrum with varying risks of hepatocellular carcinoma (HCC). Limited sample sizes limit the development of predictive models, particularly for rare outcomes. This study evaluated whether generative artificial intelligence (AI)‐based synthetic data augmentation can enhance HCC risk
Masaya Sato +12 more
wiley +1 more source
ABSTRACT Gastric perforation after endoscopic treatment of gastric fundal variceal bleeding is extremely rare. In carefully selected patients with early, small perforations and limited peritoneal contamination, endoscopic tissue adhesive injection combined with conservative management may provide a feasible nonsurgical rescue strategy.
Tianwen Liu +6 more
wiley +1 more source

